Urethane-d5(Synonyms: Ethyl carbamate-d5; Carbamic acid ethyl ester-d5; Ethylurethane-d5)

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Urethane-d5 (Synonyms: Ethyl carbamate-d5; Carbamic acid ethyl ester-d5; Ethylurethane-d5) 纯度: ≥98.0%

Urethane-d5 (Ethyl carbamate-d5) 是 Urethane 的氘代。Urethane (Ethyl carbamate) 氨基甲酸的乙酯,是多种食品中发酵的副产物。Urethane 具有抑制细菌,原生动物,海胆卵和植物组织生长的能力。

Urethane-d5(Synonyms: Ethyl carbamate-d5;  Carbamic acid ethyl ester-d5;  Ethylurethane-d5)

Urethane-d5 Chemical Structure

CAS No. : 73962-07-9

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生物活性

Urethane-d5 (Ethyl carbamate-d5) is the deuterium labeled Urethane. Urethane (Ethyl carbamate), the ethyl ester of carbamic acid, is a byproduct of fermentation found in various food products. Urethane has the ability to suppress bacterial, protozoal, sea urchin egg, and plant tissue growth in vitro[1].

体外研究
(In Vitro)

Stable heavy isotopes of hydrogen, carbon, and other elements have been incorporated into drug molecules, largely as tracers for quantitation during the drug development process. Deuteration has gained attention because of its potential to affect the pharmacokinetic and metabolic profiles of drugs[1].

Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only.

分子量

94.12

Formula

C3H2D5NO2

CAS 号

73962-07-9

中文名称

氨基甲酸乙酯 d5

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式
Powder -20°C 3 years
4°C 2 years
In solvent -80°C 6 months
-20°C 1 month
参考文献
  • [1]. Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019;53(2):211-216.

    [2]. K J Field, et al. Hazards of urethane (ethyl carbamate): a review of the literature. Lab Anim. 1988 Jul;22(3):255-62.;R E Sotomayor, et al. Mutagenicity, metabolism, and DNA interactions of urethane. Toxicol Ind Health. 1990 Jan;6(1):71-108.

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